微小亚历山大藻(Alexandrium minutum)的氮磷吸收、生长、产毒动态变化

采用浮游植物计数法、高效液相色谱串联质谱法、分光光度法等分析方法,探索了微小亚历山大藻(Alexandrium minutum)在批次培养过程中氮磷吸收、产毒、生物量、p H等参数的动态变化关系。结果表明,微小亚历山大藻对磷的吸收迅速,可以将磷储存于体内,待生长使用。该藻对氮的吸收相对缓慢,环境中氮缺乏时,产毒量不再增加,说明氮对产毒有着重要的调控作用。在第二对数期中出现了碳限制环境,导致叶绿素a在碳限制条件下无法表征藻的生物量,相反,叶绿素a和生物量呈负线性关系,可能是叶绿素转化成其它含碳物质,用于生长。毒素不仅存在于细胞体内,培养液中(胞外)也含有毒素,并且胞外毒素从稳定期开始逐渐升高。胞内毒素的组成中GTX1/4占据绝对优势,GTX2/3含量相对较少。生长延缓期和第一对数期,各种毒素组成比例相对稳定,而在随后的生长期内,GTX1/4在总毒素中的占比逐渐上升,GTX2/3占比逐渐下降,表明微小亚历山大藻毒素组成会随着生长周期的变化而发生变化。     

长三角经济高速发展地区土壤pH时空变化及其影响因素

通过调查和分析长三角地区张家港市2004年和第二次土壤普查时(1980)的土壤pH,探讨了该市近20年来基于经济高速发展影响下的土壤pH变化及影响因素。结果表明,自第二次土壤普查以来,该市土壤pH变化明显。南部人为土地区绝大部分土壤pH值都下降了一个单位,平均值由7.39降至6.33;北部雏形土区,两个时期的土壤pH值分别为7.92和7.98。土壤pH的降低可能同该地区长期施用化学肥料、酸雨及工业酸性“三废”排放的增加有关。此外,土地利用和田间管理也对土壤pH变化起着较为重要的作用,而土壤地球化学性质差异则是导致南北地区土壤pH变化不同的内在因素。     

Spatial patterns of groundwater‐lake exchange – implications for acid neutralization processes in an acid mine lake

Exchange of groundwater and lake water with typically quite different chemical composition is an important driver for biogeochemical processes at the groundwater‐lake interface, which can affect the water quality of lakes. This is of particular relevance in mine lakes where anoxic and slightly acidic groundwater mixes with oxic and acidic lake water (pH < 3). To identify links between groundwater‐lake exchange rates and acid neutralization processes in the sediments, exchange rates were quantified and related to pore‐water pH, sulfate and iron concentrations as well as sulfate reduction rates within the sediment. Seepage rates measured with seepage meters (?2.5 to 5.8 L m^‐2 d^‐1) were in reasonable agreement with rates inverted from modeled chloride profiles (?1.8 to 8.1 L m^‐2 d^‐1). Large‐scale exchange patterns were defined by the (hydro)geologic setting but superimposed by smaller scale variations caused by variability in sediment texture. Sites characterized by groundwater upwelling (flow into the lake) and sites where flow alternated between upwelling and downwelling were identified. Observed chloride profiles at the alternating sites reflected the transient flow regime. Seepage direction, as well as seepage rate, were found to influence pH, sulfate and iron profiles and the associated sulfate reduction rates. Under alternating conditions proton‐consuming processes, for example, sulfate reduction, were slowed. In the uppermost layer of the sediment (max. 5 cm), sulfate reduction rates were significantly higher at upwelling (>330 nmol g^‐1 d^‐1) compared to alternating sites (<220 nmol g^‐1 d^‐1). Although differences in sulfate reduction rates could not be explained solely by different flux rates, they were clearly related to the prevailing groundwater‐lake exchange patterns and the associated pH conditions. Our findings strongly suggest that groundwater‐lake exchange has significant effects on the biogeochemical processes that are coupled to sulfate reduction such as acidity retention and precipitation of iron sulfides. Copyright © 2012 John Wiley & Sons, Ltd.     

Characteristics of ionic components in precipitation in Kitakyushu City,Japan

Precipitation samples were collected by filtrating bulk sampler in Kitakyushu City, Japan, from January 1988 to December 1990. Volume weighted annual mean of pH was 4.93, but the pH distribution indicated that most probable value lay in the range pH 6.0–6.4. Volume weighted annual mean concentrations of major ionic components were as follows; SO ₄ ^2– : 84.2, NO ₃ ^– : 28.1, Cl^–: 86.3, NH ₄ ⁺ : 45.5, Ca²⁺: 63.3, Mg²⁺: 27.0, K⁺: 3.4, Na⁺: 69.0 µ eq l^–1. The highest concentrations of these ionic components were observed in winter and the lowest occurred in the rainy season. The ratio of ex-SO ₄ ^2– /NO ₃ ^– exhibited the lowest ratio in summer, and the highest ratio in winter. Good correlations were obtained between Cl^– and Na⁺, ex-SO ₄ ²⁺ and ex-Ca²⁺, NO ₃ ^– and ex-Ca²⁺, and NH ₄ ⁺ and ex-SO ₄ ^2– , respectively. However, no correlation between Cl^– and Na⁺ with Ca²⁺ was observed. The relationship of H⁺ with (ex-SO ₄ ^2– + NO ₃ ^– ) - (ex-Ca²⁺ + NH ₄ ⁺ ) indicated positive correlation.     

The Holocene paleolimnology of Lake Sämbosjön,southwestern Sweden

The Holocence paleolimnology of Lake Sämbosjön is described using geochemical and diatom analyses. The objective of this study is the reconstruction of major changes in trophic state and productivity, and to interpret the major causative processes. The accumulation of organic matter indicates a relatively high productivity in early Holocene, and the diatom analysis indicates a relatively high trophic state and pH. A succeeding decrease in productivity and trophic state and lowering in pH is recorded from about 8000 BP. If lake development had been primarily edaphically conditioned, viz. determined by nutrient supply from catchment soils, such a progressive oligotrophication would represent the common development of temperate lakes. Between about 6000 BP and 4000 BP Lake Sämbosjön was characterized by relatively stable productivity and pH. From about 4000 BP the analyses reveal an increase again in trophic state, productivity, and in pH. This eutrophication, which continued throughout the late Holocene, was caused by an exceptionally strong human influence on the catchment of Lake Sämbosjön. The increased supply of nutrients from cleared and deforested catchment soils changed the trophic state and provided the basis for increased lake productivity.     

How does landfill leachate affect the chemical processes in a lake system downgradient from a landfill site?

A field study on the geochemical properties of a chemically-stressed limnic environment was performed in Lake Silbersee, which receives leachate water of high inorganic loading from an upgradient landfill site. The highly concentrated sulfate ion in groundwater, when entering the pore water system of the lake, gives rise to an intensive microbial sulfate reduction. A diagenetic approach was used to explain the existence of a marine-like aqueous system within a geologically slightly acidic aquifer, consisting of a well-buffered lake water and an alkalinity producing, excess sulphide containing sediment pore water system.     

Direct and Indirect pCO2 Measurements in a Wide Range of pCO2 and Salinity Values (The Scheldt Estuary)

Recent improvements in both Infra-red spectroscopy and equilibrator techniqueshave allowed to determine, for the first time, pCO₂using simultaneously and continuously both the direct and indirect methods in an estuary where pCO₂ values range from 500 to 8500 atm and salinity from 0 to 30. Our results show that both methods are in excellent agreement in the wholeestuary (r² = 0.999, n = 1075, p < 0.0001). Thus, the NBS (US National Bureau of Standards) scale, although inadequate for seawater samples, is appropriate for estuarine waters and can be applied with confidence to calculate pCO₂.     

Influence of Temporal Variations in River Discharge, pH, Alkalinity and Ca on the Speciation and Concentration of Heavy Metals in Some Mining Polluted Rivers

Dissolved (dialysis in situ) and total concentrations ofCu, Zn, Cd and Al in eight mining polluted rivers in the Røros area, central Norway, were determinedby atomic absorption spectrometry (flame and graphite furnace) and compared to pH, Caconcentration and alkalinity through seasonal variations in river discharge. Totalconcentrations of the metals were highest during early spring flood and during summer andautumn rain episodes. Dissolved concentrations also increased as the spring floodproceeded, but small discharge peaks within this 2 month period as well as a considerableautumn flood episode appeared to lower rather than to raise the dissolved metal concentrations.Consequently the dissolved fractions of Zn, Cd and Al showed a significant negative correlationwith river discharge, and were low at the discharge peaks. Possibly high sediment concentrationsoccurring at high flood conditions more than counteracted desorption induced by pHdecrease, and led to decreased dissolved fractions through adsorption. Cu speciationon the other hand seemed to be more closely linked to pH. Alkalinity and Ca concentration,both assumed to protect aquatic life from metal pollution, were significantly lowerduring episodes with high Cu and Al total concentrations.     

Paleolimnological reconstructions of Rouyn-Noranda lakes within the zone of influence of the Horne Smelter,Québec,Canada

Diatoms were identified and enumerated from a surface sediment calibration set of 50 lakes in northwestern Québec. The relationship between species composition and environmental variables was examined using canonical correspondence analysis (CCA). Forward selection and Monte Carlo permutation tests in CCA indicated that diatom species distributions in the data set are most strongly correlated to lakewater pH. A strong (r ² _boot = 0.83) weighted averaging calibration model, that includes bootstrapped error estimates, was developed for inferring past lakewater pH. Using this model, temporal changes in pH were reconstructed for two kettle lakes, Lac de la Pépinière and Lac Perron. Based on limnological data, both the study lakes were expected to have recently acidified due to increased acidic precipitation and increases in anthropogenic metal loading. However, our long-term pH inference data indicate that these lakes were naturally acidic during pre-industrial times. Nonetheless, the rate of acidification, particularly in Lac de la Pépinière, has accelerated in the last ∼75 years. These long-term pH records developed for the dilute lakes in northwestern Québec suggest that the region has received increased atmospheric pollutants from the nearby Horne smelter in Rouyn-Noranda. The pH inference profiles are markedly different from many other paleolimnological studies in acid-sensitive regions of Canada that have become acidic primarily as a result of industrial activities. Electronic supplementary material The online version of this article (doi: ) contains supplementary material, which is available to authorized users.